Scientist

Expertise in Nitrosamine and elemental impurities and recent regulatory updates. Handling of analytical instruments e.g. HPLC, UPLC, UV, KF, Particle Size, Dissolution, LCMS, GCMS, ICPMS and Zetasizer. Expertise in Analytical Method Development Assay/ RS/CU/ Dissolution and report writing.

Monitoring of analytical functions and ensuring real-time analytical support to the cross-function team to achieve the timeline of different projects. Analytical method validation of drug substance and different dosage forms.

Doctoral degree in science or Masters degree in Engineering or Technology from a recognized University or equivalent, Doctoral degree in science or Masters Degree in Engineering or Technology from a recognized University or equivalent

Lead and mentor a team of research scientists and chemists. Oversee projects, ensuring timely, budget-friendly, and high-quality delivery. Provide expertise in solving complex synthetic challenges and optimising reactions

Ph.D. in Pharmaceutical Sciences or Analytical Chemistry, Pharmaceutical Analysis with first class post- graduation in M.Sc. Analytical Chemistry, Organic Chemistry or M.Pharm, MS.Pharm Pharmaceutical Analysis, Quality Assurance, Natural Products, Medicinal Chemistry with 60% marks.

Post Graduate degree in any of the subjects viz- Biochemistry or Chemistry or Anthropology or Sociology or Social Work or food and Nutrition or Economics with specialization in Health Economies or Psychology or Biology or Bio science or Entomology or Genetics or Medical Genetics or Immunology or Microbiology or Molecular biology or Pharmacology or Pharmacy or Toxicology

areas of life science/ medical device/pharmaceuticals/ engineering / science; Experience in the area of orthopedic, neurological, ocular implants or Biosensors or IVDs or therapeutic devices Drug-device combinations with proven track record through published high-impact research papers, patents and product development.

Responsible for timely preparation of collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs. To review the analytical data received from the Collaborators and to prepare summary reports and RSCEP packages, preparation of packaging and QC testing instructions and assigning periodic re-test intervals.

M.Sc, M.Pharm, M.V.Sc from recognized University, Institute. 2 years of experience of research, teaching in Central State Govt. Organizations, University or Research Institution or Central, State autonomous or other recognized Institute of repute.